HGVS | Genome Assembly |
---|---|
NC_000001.11:g.20645572C= , CM000663.2:g.20645572C= | GRCh38 |
NC_000001.10:g.20972065C= , CM000663.1:g.20972065C= | GRCh37 |
NC_000001.9:g.20844652C= | NCBI36 |
NG_008164.1:g.17118C= |
HGVS | Amino-acid change | |
---|---|---|
ENST00000321556.5:c.972C= (PINK1) MANE Select | ENSP00000364204.3:p.Thr324= | |
ENST00000321556.4:c.972C= (PINK1) | ENSP00000364204.3:p.Thr324= | |
ENST00000400490.2:n.65C= (PINK1) | ||
ENST00000492302.1:n.2060C= (PINK1) | ||
NM_032409.2:c.972C= (PINK1) | NP_115785.1:p.Thr324= | |
NR_046507.1:n.3981+13G= (PINK1-AS) | ||
NM_032409.3:c.972C= (PINK1) MANE Select | NP_115785.1:p.Thr324= |